Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1051550.RAUg20KH6WDJCm3FahIYwebgQUF1kBoCuLoU5dl1dzUu0130_assertion> ?p ?o ?g. }
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- NP1051550.RAUg20KH6WDJCm3FahIYwebgQUF1kBoCuLoU5dl1dzUu0130_assertion type Assertion NP1051550.RAUg20KH6WDJCm3FahIYwebgQUF1kBoCuLoU5dl1dzUu0130_head.
- NP1051550.RAUg20KH6WDJCm3FahIYwebgQUF1kBoCuLoU5dl1dzUu0130_assertion description "[These findings indicate that core myopathies are the most common form of congenital myopathies and that more than half can be attributed to RYR1 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1051550.RAUg20KH6WDJCm3FahIYwebgQUF1kBoCuLoU5dl1dzUu0130_provenance.
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- NP1051550.RAUg20KH6WDJCm3FahIYwebgQUF1kBoCuLoU5dl1dzUu0130_assertion SIO_000772 23394784 NP1051550.RAUg20KH6WDJCm3FahIYwebgQUF1kBoCuLoU5dl1dzUu0130_provenance.
- NP1051550.RAUg20KH6WDJCm3FahIYwebgQUF1kBoCuLoU5dl1dzUu0130_assertion wasDerivedFrom befree-2016 NP1051550.RAUg20KH6WDJCm3FahIYwebgQUF1kBoCuLoU5dl1dzUu0130_provenance.
- NP1051550.RAUg20KH6WDJCm3FahIYwebgQUF1kBoCuLoU5dl1dzUu0130_assertion wasGeneratedBy ECO_0000203 NP1051550.RAUg20KH6WDJCm3FahIYwebgQUF1kBoCuLoU5dl1dzUu0130_provenance.